Published in Clin Biochem on February 01, 1980
The prognostic value of serum troponin T in unstable angina. N Engl J Med (1992) 5.04
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S-troponin T in suspected ischemic myocardial injury compared with mass and catalytic concentrations of S-creatine kinase isoenzyme MB. Clin Chem (1991) 1.66
Multicenter evaluation of the Micral-Test II test strip, an immunologic rapid test for the detection of microalbuminuria. Diabetes Care (1997) 1.45
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[Toxicology of ethyleneglycol-monoethyl ether]. Arzneimittelforschung (1971) 1.35
N-acetylglutamate synthetase deficiency: a disorder of ammonia detoxication. N Engl J Med (1981) 1.31
Variants of citrullinaemia. Arch Dis Child (1973) 1.20
Urine analysis performed by flow cytometry: reference range determination and comparison to morphological findings, dipstick chemistry and bacterial culture results--a multicenter study. Clin Nephrol (2001) 1.19
Purification and properties of acetyl-CoA:L-glutamate N-acetyltransferase from human liver. Biochem J (1982) 1.12
Ultrastructural, immunocytochemical and stereological investigation of hepatocytes in a patient with the mutation of the ornithine transcarbamylase gene. Eur J Cell Biol (1995) 1.08
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N-acetylglutamate synthetase deficiency: diagnosis, management and follow-up of a rare disorder of ammonia detoxication. Eur J Pediatr (1991) 1.06
N-acetylglutamate synthetase (NAGS) deficiency: diagnosis, clinical observations and treatment. Adv Exp Med Biol (1982) 1.05
The effect of enzyme induction on diazepam metabolism in man. Br J Clin Pharmacol (1979) 1.05
Purification and properties of arginase from human liver and erythrocytes. Biochem J (1978) 1.05
A new neonatal case of N-acetylglutamate synthase deficiency treated by carbamylglutamate. J Inherit Metab Dis (1995) 1.05
Long-term follow-up of 12 patients with the late-onset variant of argininosuccinic acid lyase deficiency: no impairment of intellectual and psychomotor development during therapy. Pediatrics (1992) 1.03
Increased ratio between serum beta- and alpha-lipoproteins during diuretic therapy: an adverse effect? Clin Sci Mol Med Suppl (1978) 1.03
Early diagnosis and treatment of neonatal medium-chain acyl-CoA dehydrogenase deficiency: report of two siblings. Eur J Pediatr (1990) 1.01
N-Acetylglutamate synthetase deficiency responding to carbamylglutamate. J Inherit Metab Dis (1997) 1.01
Prenatal diagnosis of carbamoyl phosphate synthetase I deficiency by identification of a missense mutation in CPS1. Hum Mutat (1998) 0.99
L-Lysine dehydrogenase deficiency in a patient with congenital lysine intolerance. Nature (1966) 0.98
Selective deficiency of hepatic triglyceride lipase in uremic patients. N Engl J Med (1977) 0.98
Periodic attacks of lethargy in a baby with ammonia intoxication due to a congenital defect in ureogenesis. Arch Dis Child (1969) 0.97
Increased tryptophan uptake into the brain in hyperammonemia. Life Sci (1983) 0.97
Brain development: 1H magnetic resonance spectroscopy of rat brain extracts compared with chromatographic methods. Neurochem Res (1990) 0.97
[Hyperargininemia wityh arginase deficiency. A new familial metabolic disease. I. Clinical studies]. Z Kinderheilkd (1970) 0.97
Incidence of disorders tested by systematic screening: confidence limits and comparison of programmes. J Inherit Metab Dis (1982) 0.96
Chronic renal magnesium loss, hypocalciuria and mild hypokalaemic metabolic alkalosis after cisplatin. Pediatr Nephrol (1990) 0.94
Enzyme induction and renal function in man. Br J Clin Pharmacol (1977) 0.94
Familial hyperargininaemia. Arch Dis Child (1975) 0.93
Enhanced synthesis of albumin and fibrinogen at high altitude. J Appl Physiol (1985) (2001) 0.93
Phenylketonuria, a family study. Borderline intelligence in two siblings with mentally retarded children. Helv Paediatr Acta (1967) 0.92
[The effect of diuretic therapy on serum lipoproteins: an undesirable effect?]. Schweiz Med Wochenschr (1979) 0.91
Diagnostic value of orotic acid excretion in heritable disorders of the urea cycle and in hyperammonemia due to organic acidurias. Eur J Pediatr (1980) 0.91
Ornithine transcarbamylase deficiency: new sites with increased probability of mutation. Hum Genet (1995) 0.91
Ornithine transcarbamylase deficiency: characterization of gene mutations and polymorphisms. Hum Mutat (1996) 0.90
Increased serum low-density lipoprotein cholesterol in men treated short-term with the diuretic chlorthalidone. Metabolism (1980) 0.90
Guanidino compound analysis as a complementary diagnostic parameter for hyperargininemia: follow-up of guanidino compound levels during therapy. Pediatr Res (1990) 0.90
Diuretic treatment and serum lipoproteins: effects of tienilic acid and indapamide. Klin Wochenschr (1981) 0.89
Effect of enzyme induction on plasma lipids using antipyrine, phenobarbital, and rifampicin. Clin Pharmacol Ther (1979) 0.89
Isolation and identification of the urinary pigment uroerythrin. Eur J Biochem (1975) 0.88
Extracellular magnesium depletion in pediatric patients with insulin-dependent diabetes mellitus. Miner Electrolyte Metab (1997) 0.88
Prenatal diagnosis of the urea cycle diseases: a survey of the European cases. Am J Med Genet (1995) 0.86
Increase of tryptophan and 5-hydroxyindole acetic acid in the brain of ornithine carbamoyltransferase deficient sparse-fur mice. Pediatr Res (1984) 0.86
Enzymatic determination of red cell creatine as an index of hemolysis. Clin Biochem (1987) 0.86
Determination of orotic acid in children's urine. J Clin Chem Clin Biochem (1980) 0.85
Unsuccessful trial of gene replacement in arginase deficiency. Z Kinderheilkd (1975) 0.85
Glutaric aciduria type I: ultrasonographic demonstration of early signs. Pediatr Radiol (1999) 0.85
[The determination of bilirubin as azobilirubin in plasma and serum with the Greiner electronic selective analyzer GSA II (author's transl)]. Z Klin Chem Klin Biochem (1974) 0.83
The renal handling of carnitine in patients with selective tubulopathy and with Fanconi syndrome. Pediatr Res (1987) 0.83
Late-onset form of partial N-acetylglutamate synthetase deficiency. Eur J Pediatr (1990) 0.82
N-acetylglutamate synthetase deficiency, a second patient. J Inherit Metab Dis (1988) 0.82
Impact of chronic cigarette smoking on body composition and fuel metabolism. J Clin Endocrinol Metab (1995) 0.82
[Hyperargininemia with arginase deficiency. A new familial metabolic disease. II. Biochemical studies]. Z Kinderheilkd (1970) 0.82
[Wilson's disease in Switzerland. Clinical, genetic and biochemical studies]. Schweiz Med Wochenschr (1973) 0.82
Carbamyl phosphate synthetase-1 deficiency discovered after valproic acid-induced coma. Acta Neurol Scand (1992) 0.81
[Periodic stupor and ammonia intoxication in a child with anicteric subacute hepatitis]. Helv Paediatr Acta (1967) 0.81
[Hyperammonemia due to ornithine transcarbamylase deficiency--a cause of lethal metabolic crisis during the newborn period and infancy (author's transl)]. Klin Padiatr (1980) 0.81
Partial N-acetylglutamate synthetase deficiency: a new case with uncontrollable movement disorders. J Inherit Metab Dis (1992) 0.81
Cardiovascular and renal profile of acute peripheral dopamine1-receptor agonism with fenoldopam. Hypertension (1987) 0.81
Methylmalonic acidaemia and nonketotic hyperglycinaemia. Clinical and biochemical aspects. Arch Dis Child (1975) 0.81
Effect of L-dopa on visual evoked potentials and neuropsychological tests in adult phenylketonuria patients. Eur J Pediatr (1996) 0.80
[Heavy chain disease. A case of IgG-heavy-chain-fragment and IgM-type K-paraproteinemia with plasma cell leukemia]. Schweiz Med Wochenschr (1970) 0.79
The defect of uric acid metabolism in Eck-fistula rats. J Lab Clin Med (1977) 0.79
In vivo 31P NMR spectroscopy of energy rich phosphates in the brain of the hyperammonemic rat. Biochem Biophys Res Commun (1989) 0.79
Excretion of different substances in the sweat of children with cystic fibrosis and controls. Bibl Paediatr (1967) 0.79
[Late diagnosis of congenital argininemia during administration of sodium valproate]. Rev Neurol (Paris) (1990) 0.79
Effect of L-dopa on pattern visual evoked potentials (P-100) and neuropsychological tests in untreated adult patients with phenylketonuria. J Inherit Metab Dis (1994) 0.78
3-Hydroxy-3-methylglutaryl-CoA-lyase deficiency. J Inherit Metab Dis (1989) 0.78
[The determination of glucose in plasma and serum (hexokinase-glucose-6-phosphate dehydrogenase method) with the Greiner electronic selective analyzer GSA II (author's transl)]. Z Klin Chem Klin Biochem (1974) 0.78
[The treatment of hyperuricemia after kidney transplantation]. Schweiz Med Wochenschr (1977) 0.78
[Wilson's disease in Switzerland. Clinical, genetic and biochemical studies]. Schweiz Med Wochenschr (1973) 0.78
Brain uptake of tryptophan in urease-injected hyperammonemic rats after treatment with benzoate or hippurate. Biochem Med Metab Biol (1986) 0.78
Sweat composition in relation to rate of sweating in patients with cystic fibrosis of the pancreas. Pediatr Res (1968) 0.78
Plasma ammonia concentrations in newborns and children. Clin Chim Acta (1984) 0.78
[Osteomalacia due to a long-term antiepileptic treatment]. Schweiz Med Wochenschr (1972) 0.78
Increased plasma amylase in the family of a patient with 3-hydroxy-3-methylglutaryl-coenzyme A lyase deficiency. Clin Chem (1992) 0.78
Plasma glutamine in a phenylketonuric family with normal and mentally defective members. Arch Dis Child (1971) 0.78
Free circulating magnesium and renal magnesium handling during acute metabolic acidosis in humans. Am J Nephrol (1998) 0.77
Determination of thiocyanate in plasma and saliva without deproteinisation and its validation as a smoking parameter. J Clin Chem Clin Biochem (1987) 0.77
[Fructosamine determination as a screening test for diabetes mellitus in patients with acute coronary heart disease]. Schweiz Med Wochenschr (1988) 0.77
Short chain fatty acids in plasma and brain: quantitative determination by gas chromatography. Clin Chim Acta (1979) 0.77
Clinical and biochemical findings in argininemia. Adv Exp Med Biol (1982) 0.77
Stimulation of tryptophan uptake into brain microvessels by D-glutamine. Brain Res (1986) 0.77
Hypermagnesiuria in children with newly diagnosed insulin-dependent diabetes mellitus. Am J Nephrol (1994) 0.77
Inborn defects of the mitochondrial portion of the urea cycle. Ann N Y Acad Sci (1986) 0.77
Lethal osteogenesis imperfecta: abnormal collagen metabolism and biochemical characteristics of hypophosphatasia. Eur J Pediatr (1988) 0.77
Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome: low creatine excretion and effect of citrulline, arginine, or ornithine supplement. Pediatr Res (1987) 0.77
Effect of increasing dietary threonine intakes on amino acid metabolism of the central nervous system and peripheral tissues in growing rats. Pediatr Res (1998) 0.77
Familial hyperargininemia. J Genet Hum (1972) 0.77
Creatine kinase and creatine kinase MB in endurance runners and in patients with myocardial infarction. Eur J Appl Physiol Occup Physiol (1985) 0.77
Identification of four novel splice site mutations in the ornithine transcarbamylase gene. Hum Genet (1996) 0.77
[The diagnostic value of alkaline phosphatase, leucine aminopeptidase and gamma-glutamytranspeptidase in diseases of the biliary tract]. Schweiz Med Wochenschr (1968) 0.76
Congenital disorders of the urea cycle and ammonia detoxication. Monogr Paediatr (1971) 0.76